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Journal of Inherited Metabolic Disease|January 1, 1987
A sibship with a mild variant of Zellweger syndromeP G Barth, R B Schutgens, R J Wanders, et al.American Journal of Medical Genetics. Part A|May 12, 2005
Cerebral, cerebellar, and colobomatous anomalies in three related males: Sex-linked inheritance in a newly recognized syndrome with features overlapping with Joubert syndromeHester Y Kroes, Rutger-Jan A J Nievelstein, Peter G Barth, et al.Neurology|February 12, 2004
Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survivalP G Barth, C B L M Majoie, J Gootjes, et al.Journal of Inherited Metabolic Disease|August 20, 2015
Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthoodKevin Berendse, Marc Engelen, Sacha Ferdinandusse, et al.AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.Human Mutation|August 21, 2008
Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell linesMerel S Ebberink, Petra A W Mooyer, Janet Koster, et al.Neuropediatrics|June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruptionH L M van Straaten, J P van Tintelen, J M F Trijbels, et al.American Journal of Medical Genetics. Part A|April 21, 2004
Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patientsBwee Tien Poll-The, Jeannette Gootjes, Marinus Duran, et al.Brain : a Journal of Neurology|August 11, 2007
Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidancePeter G Barth, Charles B Majoie, Matthan W A Caan, et al.Human Mutation|July 17, 1999
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disordersZ Zhang, Y Suzuki, N Shimozawa, et al.Pageof 30